CN1033226C - 烷氧基链烷酸的制备 - Google Patents
烷氧基链烷酸的制备 Download PDFInfo
- Publication number
- CN1033226C CN1033226C CN91110929A CN91110929A CN1033226C CN 1033226 C CN1033226 C CN 1033226C CN 91110929 A CN91110929 A CN 91110929A CN 91110929 A CN91110929 A CN 91110929A CN 1033226 C CN1033226 C CN 1033226C
- Authority
- CN
- China
- Prior art keywords
- nitroxide
- group
- dissolved
- tetramethyl
- alkoxyalkanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000002253 acid Substances 0.000 title claims abstract description 29
- 238000002360 preparation method Methods 0.000 title abstract description 3
- 150000007513 acids Chemical class 0.000 title description 13
- 238000000034 method Methods 0.000 claims abstract description 31
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims abstract description 29
- 239000007800 oxidant agent Substances 0.000 claims abstract description 21
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 14
- -1 alkyl nitroxide Chemical group 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
- 150000003839 salts Chemical class 0.000 claims abstract description 7
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 18
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 15
- 239000000203 mixture Chemical group 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- 239000000460 chlorine Substances 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims description 8
- 238000007254 oxidation reaction Methods 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000011541 reaction mixture Substances 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 230000003647 oxidation Effects 0.000 claims description 7
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- QYTDEUPAUMOIOP-UHFFFAOYSA-N TEMPO Chemical group CC1(C)CCCC(C)(C)N1[O] QYTDEUPAUMOIOP-UHFFFAOYSA-N 0.000 claims description 3
- AEMWMKZASFWBGX-UHFFFAOYSA-N 2,2,3,3-tetrachlorooxepane Chemical compound ClC1(Cl)CCCCOC1(Cl)Cl AEMWMKZASFWBGX-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 238000002955 isolation Methods 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 abstract description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 238000002156 mixing Methods 0.000 abstract description 2
- 150000003254 radicals Chemical class 0.000 description 17
- 235000019441 ethanol Nutrition 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 5
- 239000005708 Sodium hypochlorite Substances 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000003599 detergent Substances 0.000 description 5
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- VUZNLSBZRVZGIK-UHFFFAOYSA-N 2,2,6,6-Tetramethyl-1-piperidinol Chemical group CC1(C)CCCC(C)(C)N1O VUZNLSBZRVZGIK-UHFFFAOYSA-N 0.000 description 3
- UZFMOKQJFYMBGY-UHFFFAOYSA-N 4-hydroxy-TEMPO Chemical group CC1(C)CC(O)CC(C)(C)N1[O] UZFMOKQJFYMBGY-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- JWUXJYZVKZKLTJ-UHFFFAOYSA-N Triacetonamine Chemical compound CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical class O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- WSGDRFHJFJRSFY-UHFFFAOYSA-N 4-oxo-TEMPO Chemical group CC1(C)CC(=O)CC(C)(C)N1[O] WSGDRFHJFJRSFY-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 1
- YLFIGGHWWPSIEG-UHFFFAOYSA-N aminoxyl Chemical compound [O]N YLFIGGHWWPSIEG-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/29—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with halogen-containing compounds which may be formed in situ
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/618,205 US5175360A (en) | 1990-11-26 | 1990-11-26 | Preparation of alkoxyalkanoic acids |
| US618,205 | 1990-11-26 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1061773A CN1061773A (zh) | 1992-06-10 |
| CN1033226C true CN1033226C (zh) | 1996-11-06 |
Family
ID=24476759
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN91110929A Expired - Fee Related CN1033226C (zh) | 1990-11-26 | 1991-11-22 | 烷氧基链烷酸的制备 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US5175360A (de) |
| EP (1) | EP0488467B1 (de) |
| JP (1) | JP3101037B2 (de) |
| KR (1) | KR100218651B1 (de) |
| CN (1) | CN1033226C (de) |
| AU (1) | AU643339B2 (de) |
| BR (1) | BR9105080A (de) |
| CA (1) | CA2055804C (de) |
| DE (1) | DE69116826T2 (de) |
| ES (1) | ES2083516T3 (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108659213A (zh) * | 2018-06-22 | 2018-10-16 | 南京工业大学 | 一种采用微流场反应技术制备聚醚羧酸盐的方法 |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5292940A (en) * | 1989-09-01 | 1994-03-08 | Henkel Kommanditgesellschaft Auf Aktien | Process for the preparation of alkali metal salts of ether-carboxylic acids |
| US5334756A (en) * | 1991-03-26 | 1994-08-02 | Sandoz Ltd. | Carboxylate of certain polyoxyalkylene amines |
| US5387712A (en) * | 1992-11-24 | 1995-02-07 | Shell Oil Company | Preparation of aromatic alkoxyalkanoic acids |
| US5250727A (en) * | 1992-12-23 | 1993-10-05 | Shell Oil Company | Preparation of alkoxyalkanoic acids |
| US5401874A (en) * | 1993-03-04 | 1995-03-28 | Shell Oil Company | Preparation of alkoxyalkanoic acids |
| US5336811A (en) * | 1993-08-18 | 1994-08-09 | Shell Oil Company | Process for the preparation of aldehydes |
| US5380930A (en) * | 1993-12-17 | 1995-01-10 | Shell Oil Company | Process for the preparation of alkoxyalkanoic acids |
| US5391822A (en) * | 1993-12-22 | 1995-02-21 | Shell Oil Company | Process for the preparation of branched alkoxyalkanoic acids |
| US5352824A (en) * | 1993-12-22 | 1994-10-04 | Shell Oil Company | Process for the preparation of alkoxyalkanoic acids |
| DE4415062B4 (de) * | 1994-04-29 | 2004-04-01 | Stockhausen Gmbh & Co. Kg | Mittel und Verfahren zur Hydrophobierung von Ledern und Pelzen |
| US5488154A (en) * | 1994-10-13 | 1996-01-30 | Shell Oil Company | Process for the preparation of alkoxyalkanoic acids |
| US5495045A (en) * | 1994-12-22 | 1996-02-27 | Shell Oil Company | Process for the preparation of alkoxyalkanoic acids |
| US5608106A (en) * | 1995-05-11 | 1997-03-04 | Shell Oil Company | Preparation of alkoxyalkanoic acids |
| US5608107A (en) * | 1995-05-31 | 1997-03-04 | Shell Oil Company | Preparation of alkoxyalkanoic acids |
| NL1000495C2 (nl) * | 1995-06-02 | 1996-12-03 | Avebe Coop Verkoop Prod | Geoxideerde polymere koolhydraatethers voor toepassing als sequestreer- middel, alsmede werkwijzen ter bereiding daarvan. |
| US5681903A (en) * | 1995-12-20 | 1997-10-28 | Shell Oil Company | Process for the preparation of polymeric alpha, omega-dialdehydes and diacids |
| US6235931B1 (en) | 1998-12-30 | 2001-05-22 | Shell Oil Company | Partial oxidation of polyoxyalkylene polyol compositions to polycarboxylic acid compositions |
| US20070299269A1 (en) * | 2006-06-27 | 2007-12-27 | Conopco, Inc., D/B/A Unilever | Process for converting primary amidoalcohols to amidocarboxylic acids in high yield |
| US7307187B1 (en) * | 2006-06-27 | 2007-12-11 | Conopco, Inc. | Process for converting primary amidoalcohols to amidocarboxylic acids in high yield |
| CN105503637A (zh) * | 2016-01-22 | 2016-04-20 | 江南大学 | 一种合成脂肪酰基甘氨酸的方法 |
| CN114075106B (zh) * | 2020-08-12 | 2023-09-12 | 广东省稀有金属研究所 | 一种脂肪醇醚羧酸的制备方法 |
| CN115872859A (zh) * | 2021-09-28 | 2023-03-31 | 佳化化学(上海)有限公司 | 一种醇醚羧酸的制备方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4233460A (en) * | 1979-05-03 | 1980-11-11 | Shell Oil Company | Alkoxyalkanoic acid preparation |
| DE3264875D1 (en) * | 1981-04-21 | 1985-08-29 | Mitsubishi Gas Chemical Co | Process for producing carboxylic acids |
| DE3871014D1 (de) * | 1987-07-14 | 1992-06-17 | Ciba Geigy Ag | Hydroxyaethercarbonsaeuren und ihre lactone, verfahren zu deren herstellung und ihre verwendung als korrosionsinhibitor. |
| JPH0596516A (ja) * | 1991-10-11 | 1993-04-20 | Toyota Motor Corp | 微細片の成形方法及び成形装置 |
-
1990
- 1990-11-26 US US07/618,205 patent/US5175360A/en not_active Expired - Lifetime
-
1991
- 1991-11-21 KR KR1019910020819A patent/KR100218651B1/ko not_active Expired - Fee Related
- 1991-11-22 CN CN91110929A patent/CN1033226C/zh not_active Expired - Fee Related
- 1991-11-22 EP EP91203068A patent/EP0488467B1/de not_active Expired - Lifetime
- 1991-11-22 JP JP03332937A patent/JP3101037B2/ja not_active Expired - Lifetime
- 1991-11-22 BR BR919105080A patent/BR9105080A/pt not_active IP Right Cessation
- 1991-11-22 CA CA002055804A patent/CA2055804C/en not_active Expired - Lifetime
- 1991-11-22 ES ES91203068T patent/ES2083516T3/es not_active Expired - Lifetime
- 1991-11-22 AU AU88061/91A patent/AU643339B2/en not_active Expired
- 1991-11-22 DE DE69116826T patent/DE69116826T2/de not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108659213A (zh) * | 2018-06-22 | 2018-10-16 | 南京工业大学 | 一种采用微流场反应技术制备聚醚羧酸盐的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3101037B2 (ja) | 2000-10-23 |
| AU643339B2 (en) | 1993-11-11 |
| CN1061773A (zh) | 1992-06-10 |
| KR920009765A (ko) | 1992-06-25 |
| CA2055804C (en) | 2002-06-04 |
| KR100218651B1 (ko) | 1999-09-01 |
| EP0488467A2 (de) | 1992-06-03 |
| CA2055804A1 (en) | 1992-05-27 |
| EP0488467A3 (en) | 1992-10-28 |
| DE69116826T2 (de) | 1996-09-19 |
| AU8806191A (en) | 1992-05-28 |
| ES2083516T3 (es) | 1996-04-16 |
| JPH04283537A (ja) | 1992-10-08 |
| EP0488467B1 (de) | 1996-01-31 |
| BR9105080A (pt) | 1992-06-23 |
| US5175360A (en) | 1992-12-29 |
| DE69116826D1 (de) | 1996-03-14 |
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